Moncada S, Gryglewski R J, Bunting S, Vane J R
Prostaglandins. 1976 Nov;12(5):715-37. doi: 10.1016/0090-6980(76)90048-4.
Microsomal fractions from arterial walls of pigs and rabbits and fundus of rat stomach generate from prostaglandin endoperoxides (PGG2 or H2) an unstable substance, prostaglandin X (PGX) which is a potent inhibitor of platelet aggregation induced by several different substances. Other microsomal fractions including corpus of stomach, lung and ram seminal vesicles generate smaller amounts of PGX from PGG2 or PGH2. Incubation of microsomes from arterial wall or fundus of stomach with platelet-rich plasma under various conditions shows that the enzyme which generates PGX can utilize endoperoxides liberated from platelets or added to the cuvette, thereby preventing, interrupting or reversing the process of platelet aggregation. The generation of PGX is strongly inhibited (IC50 0.43 mug/ml) by 15-hydroperoxy arachidonic acid. These observations are important in the interpretation of vascular diseases such as atherosclerosis and thrombosis and provide a rational basis for the use of anti-oxidants in the prevention and treatment of these diseases.
猪、兔动脉壁以及大鼠胃底部的微粒体部分可从前列腺素内过氧化物(PGG2或H2)生成一种不稳定物质——前列腺素X(PGX),它是几种不同物质诱导的血小板聚集的强效抑制剂。包括胃体、肺和公羊精囊在内的其他微粒体部分从PGG2或PGH2生成的PGX量较少。在各种条件下,将动脉壁或胃底部的微粒体与富含血小板的血浆一起孵育表明,生成PGX的酶可以利用从血小板释放或添加到比色皿中的内过氧化物,从而预防、中断或逆转血小板聚集过程。15-氢过氧花生四烯酸强烈抑制(IC50为0.43微克/毫升)PGX的生成。这些观察结果对于解释动脉粥样硬化和血栓形成等血管疾病很重要,并为在这些疾病的预防和治疗中使用抗氧化剂提供了合理依据。